Composition for preventing atherosclerosis

ABSTRACT

The present invention provides a composition obtained by organic solvent extraction of defatted plant seed which is an atherosclerosis preventative agent. The present invention further provides a food and a pharmaceutical composition containing the composition, as well as a method of preventing an atherosclerotic disease.

CROSS-REFERENCE TO RELATED APPLICATIONS

The present application is a continuation of International ApplicationPCT/JP03/04607, filed on Apr. 11, 2003, which claims priority toJapanese application JP 2002-110932, filed on Apr. 12, 2002, the entirecontents of these applications is incorporated herein by reference intheir entirety.

BACKGROUND OF THE INVENTION

1. Field of the Invention

The present invention provides a composition obtained by organic solventextraction of defatted plant seed which is an atherosclerosispreventative agent. The present invention further provides a food and apharmaceutical composition containing the composition, as well as amethod of preventing an atherosclerotic disease.

2. Discussion of the Background

Along with the westernization of life style in recent years, in additionto cancer, atherosclerotic diseases such as angina pectoris,intermittent claudication, cardiac infarction, cerebral infarction andthe like have become the main causes of death of Japanese people. Oncedeveloped, these diseases are very difficult to cure, and dramaticallydegrade “quality of life.” It is undisputable that a countermeasure toprevent or control the progression of atherosclerotic diseases isextremely important from a social standpoint as well.

A consensus has been generally reached that oxidation of low densitylipoprotein (LDL) plays a key role in the early stages of lesionformation. As such, the importance of not only controlling the bloodcholesterol level to a suitable range but also suppressing theproduction of oxidized LDL has been recently noted. It has beendetermined that certain foods, particularly a food derived from plants,contain an abundance of anti-oxidative substances. To this end, theanti-oxidative substances contained in green tea and red wine areconsidered to be taken into LDL (or in the vicinity thereof) andeliminate radical to prevent production of oxidized LDL (Fuhrman et al,Am. J. Clin. Nutr., 61: pp 549-54, 1995). There is also anepidemiological study that concludes that positive intake of these foodssuppress cancer and heart diseases (Renaud et al, Lancet, 339: pp1523-26, 1992).

In the meantime, there is a report that particular components derivedfrom particular seeds such as sesame seed lignan, grapeseed polyphenoland the like show an anti-atherosclerotic activity with experimentalanimals (Kang et al. J. Nutr., 129: pp 1885-90, 1999; Yamakoshi et al,Atherosclerosis 142: pp 139-49, 1999). However, the anti-atheroscleroticproperty of a plant seed component has only been determined at an animaltest level in a few cases, and many researches remain at a test tubelevel.

For example, JP-A-8-337536 discloses an anti-active oxygen agentextracted from a roasted and then fermented plant seed. The techniquedescribed in JP-A-8-337536 uses a plant seed as a starting material, buthas low versatility because it requires operations such as roasting,fermentation treatment and the like, and, thus, this technique is notpractical. In addition, no evidence exists that a fermented plant seedobtained by this method has an effect on suppressing atherosclerosis.

In another study, Zhang et al (Chem. Pharm. Bull., 45: pp 1910-14, 1997)report structures of a group of compounds extracted from a safflower oilcake by distribution of various solvents, and that some of thesestructures have an antioxidant activity in vitro. However, it is notclear at present if such compounds having an antioxidant activity areeffective for preventing atherosclerosis. In consideration of the factthat antioxidant activity in vitro is known not to be necessarilycorrelated to the anti-atherosclerotic activity in living organisms(Fruebis et al, J. Lipid Res., 38: pp 2455-64, 1997, Fruebis et al,Atherosclerosis 117: pp 217-24, 1995, Munday et al, Arterioscler.Thromb. Vasc. Biol., 18: pp 114-19, 1998, Wagberg et al, J. Pharmacol.Exp. Ther., 299: pp 76-82, 2001), confirmation of whether or not ananti-oxidative substance in a plant seed has anti-atheroscleroticproperty is required at least at an experimental animal level.

Therefore, in view of the state of the art and the ever increasingmedical concerns over atherosclerotic diseases, there remains a criticalneed for compositions that are effective atherosclerotic diseasepreventatives.

SUMMARY OF THE INVENTION

An object of the present invention is to provide a composition effectivefor preventing atherosclerosis, which is one of the lifestyle-relateddiseases. A further object of the present invention is to provide a foodand a pharmaceutical composition containing this composition. In yet afurther object of the present invention is to provide a method forpreventing atherosclerosis.

The present inventors have conducted intensive studies to achieve theabove-mentioned objects and have produced that a composition extractedwith organic solvent from defatted plant seeds that has antioxidantactivity in vitro and atherosclerosis preventive activity inexperimental animals. On the basis of these findings, the presentinvention has been completed.

Thus, the present invention provides the following.

(1) A composition for preventing atherosclerosis, comprising an organicsolvent extraction of a defatted plant seed.

(2) The composition of (1), wherein the plant seed is a seed ofsafflower.

(3) The composition of (1), wherein the plant seed is a seed ofrapeseed.

(4) The composition of (1), wherein the organic solvent extraction isobtained by a process comprising extracting a defatted plant seed with alower alcohol.

(5) The composition of (4), wherein said lower alcohol is ethanol ormethanol.

(6) The composition of (4), wherein said process further comprises,after said extracting with a lower alcohol, evaporating said loweralcohol, adding water, extracting an aqueous phase, and washing saidaqueous phase with a nonpolar solvent.

(7) The composition of (6), wherein said lower alcohol is ethanol ormethanol.

(8) The composition of (4), wherein said process further comprisesextracting with an acetate ester after said extracting with a loweralcohol.

(9) The composition of (8), wherein said acetate ester is selected fromthe group consisting of ethyl acetate, methyl acetate, and propylacetate.

(10) The composition of (6), wherein said nonpolar solvent is n-hexane.

(11) The composition of (8), wherein said lower alcohol is ethanol ormethanol.

(12) The composition of (8), wherein said process further comprises,after said extracting with a lower alcohol, evaporating said loweralcohol, adding water, extracting an aqueous phase, and washing saidaqueous phase with a nonpolar solvent.

(13) The composition of (12), wherein said lower alcohol is ethanol ormethanol.

(14) The composition of (12), wherein said acetate ester is selectedfrom the group consisting of ethyl acetate, methyl acetate, and propylacetate.

(15) The composition of (12), wherein said nonpolar solvent is n-hexane.

(16) A food comprising the composition of (1).

(17) A pharmaceutical composition comprising the composition of (1) anda pharmaceutically acceptable carrier.

(18) A method of preventing one or more atherosclerotic diseasecomprising administering to a subject in need thereof a composition of(1).

(19) The method of (18), wherein said atherosclerotic disease is one ormore selected from the group consisting of angina pectoris, cardiacinfarction, intermittent claudication, and cerebral infarction.

(20) The method of (18), wherein said effective amount ranges from 10 mgto 10 g per day.

The above objects highlight certain aspects of the invention. Additionalobjects, aspects and embodiments of the invention are found in thefollowing detailed description of the invention.

BRIEF DESCRIPTION OF THE FIGURES

A more complete appreciation of the invention and many of the attendantadvantages thereof will be readily obtained as the same becomes betterunderstood by reference to the following Figures in conjunction with thedetailed description below.

FIG. 1 shows the effect on LDL oxidation for each sample described inExample 1.

FIG. 2 shows the suppressive effect of a safflower meal extractcomposition and a rapeseed meal extract composition on atherosclerosisin the aorta of apoE (−/−) mice [atherosclerosis model mice] at week 5of administration (14-week-old mice) as described in Example 2, wherein(a) is a control group, (b) is a safflower group and (c) is a rapeseedgroup.

FIG. 3 shows a sketch of FIG. 2, wherein (a-1) is a sketch of FIG. 2(a),(b-1) is a sketch of FIG. 2(b), (c-1) is a sketch of FIG. 2(c). Thephotograph of FIG. 2 is originally a color photograph and the partstained in red shows an atheromatous plaque. FIG. 3 is a sketch for thepurpose of clarifying the red stained part in FIG. 2 by drawing a figureof FIG. 2 and blacked out the red stained part.

FIG. 4 shows an oxidation curve of LDL induced by the addition of V70(lipid peroxide producing curve).

FIG. 5 shows an aortic root lesion area in apoE knockout mice(21-week-old, male, week 15 of administration of each sample) asdescribed in Example 3, wherein SFM is a safflower meal extractcomposition, CS is p-coumaroylserotonin and FS is feruloylserotonin.

DETAILED DESCRIPTION OF THE INVENTION

Unless specifically defined, all technical and scientific terms usedherein have the same meaning as commonly understood by a skilled artisanin enzymology, biochemistry, cellular biology, molecular biology, andthe medical sciences.

All methods and materials similar or equivalent to those describedherein can be used in the practice or testing of the present invention,with suitable methods and materials being described herein. Allpublications, patent applications, patents, and other referencesmentioned herein are incorporated by reference in their entirety. Incase of conflict, the present specification, including definitions, willcontrol. Further, the materials, methods, and examples are illustrativeonly and are not intended to be limiting, unless otherwise specified.

The plant seed to be used in the present invention may be a seed of anyplant. For example, seeds of safflower, rapeseed, soybean and the likecan be mentioned, with preference given to the seeds of safflower andrapeseed. In the present invention, the term “plant seed” means thewhole constituting a plant seed, or a part thereof, such as seed coat,albumen, germ and the like, or a mixture thereof.

In the present invention, the starting material is a plant seed afterdefatting or defatted material (meal). A defatted material of plant seedcan be obtained by delipidating a plant seed by a method known per se.For example, the defatted material can be obtained by press-extractingseed or adding n-hexane and the like to a crushed seed, extracting themixture, taking out a solid content from the extraction system anddrying the solid content. The degree of defatting is generally not lessthan 60%, preferably not less than 80%.

The “organic solvent extraction” used in the present specification isexplained below. Examples of the solvent to be used in the first stepfor extracting (e.g., organic solvent extraction) from defatted seed inthe present invention include, but are not limited to, a lower alcohol(including water-containing lower alcohol), acetone (includingwater-containing acetone), acetonitrile (including water-containingacetonitrile), a mixed solvent thereof and the like. Preferably, thesolvent for extraction is a lower alcohol. In this context, loweralcohol includes, for example, an alcohol having 1 to 4 carbon atoms.Specific examples thereof include, but are not limited to, methanolethanol n-propanol isopropanol n-butanol and the like. The lower alcoholis preferably ethanol or methanol (including water-containing ethanol(e.g., 90 vol %) and water-containing methanol). A composition extractedwith such solvent is useful as a composition of the present invention ata purity thereof, but may be processed to have a higher purity (may bepurified).

One example for increasing the purity (purifying) is described in thefollowing, but the method is not limited thereto. An organic solvent ofthe above-mentioned solvent extraction is evaporated (particularlyevaporated under reduced pressure), water is added to the obtainedextract to suspend the same, the suspension (aqueous phase) is washedwith a nonpolar solvent (e.g., such as n-hexane, n-heptane, n-octane andthe- like, preferably n-hexane), and the aqueous layer after washing isextracted with a solvent that can extract an object composition in twoseparate layers (e.g., such as acetate ester, n-butanol and the like,preferably acetate ester, particularly preferably ethyl acetate, methylacetate or propyl acetate). Then, the extract is washed with saturatedbrine and the like to produce an organic layer. When it is extractedwith acetate ester, the organic layer is dehydrated over, for example,anhydrous magnesium sulfate and the like, and then concentrated underreduced-pressure to give a solid (composition). Purification may bestopped during any of the above-mentioned steps. In addition, any stepmay be omitted or modified and the purification may be repeated or stepsadded thereto. A multi-step extraction method, a counter currentdistribution method and the like can be also used, including changingthe kind of the above-mentioned solvent.

When the composition of the present invention obtained by theabove-mentioned method is used as a food or a pharmaceutical agent(atherosclerosis preventive agent etc.), and/or when the composition ispresent in a physiologically harmful solvent, the composition may bedried, or the dry product is dissolved, suspended or emulsified in aphysiologically acceptable solvent before use. The composition of thepresent invention may be in a liquid form (e.g., an aqueous solution andthe like), a solid form obtained by concentration under reduced pressureand drying, or a solidified product such as a lyophilized product andthe like.

The composition for preventing atherosclerosis of the present inventionsuppresses oxidation of LDL (low density lipoprotein) in human plasma invitro. Particularly, a composition obtained from the seed of safflowerand rapeseed strongly suppresses LDL oxidation. What is to beparticularly noted is that the composition of the present inventionsuppresses formation of atheromatous plaque on an inner wall of theblood vessels in mouse in vivo and showed an anti-atheroscleroticactivity in experimental animal. From the above, the composition of thepresent invention is useful as a pharmaceutical agent for prevention ofatherosclerosis and the like, as well as a food for preventingatherosclerosis.

The composition of the present invention prevents atherosclerosis and isuseful for preventing diseases caused by atherosclerosis, such as anginapectoris, cardiac infarction, intermittent claudication, cerebralinfarction and the like.

The “food” of the present invention means food in general, and includesgeneral food including health food, Food for Specified Health Use andFood with Nutrient Function Claims as defined in the Food with HealthClaims System of the Health, Labor and Welfare Ministry, and encompassessupplements.

As the food or pharmaceutical composition, the above-mentionedcomposition of the present invention can be used may be used withoutfurther modification. In addition, it is possible to use theabove-mentioned composition of the present invention contained invarious foods. Examples of suitable foods include a general food(including what is called health food) such as dressing, mayonnaise andthe like. Moreover, the composition of the present invention can beprepared into tablet, pill, granule, fine granules, powder, pellet,capsule, solution, emulsion, suspension, syrup, troche and the liketogether with excipients (e.g., lactose, sucrose, starch etc.), and withflavoring, dye and the like, and used as Food with Health Claims such asFood for Specified Health Use, Food with Nutrient Function Claims andthe like, supplement, pharmaceutical preparation (pharmaceuticalcomposition) (mainly for oral use).

Particularly, in the case of a pharmaceutical composition, thecomposition can be prepared along with a pharmaceutically acceptablecarrier (including additive). Examples of the pharmaceuticallyacceptable carrier include, but not limited to, excipients (e.g.,lactose, sucrose, starch, D-mannitol etc.), binders (e.g., cellulose,sucrose, dextrin, hydroxypropyl cellulose, polyvinylpyrrolidone etc.),disintegrants (e.g., starch, carboxymethyl cellulose etc.), lubricants(e.g., magnesium stearate etc.), surfactants (e.g., sodium laurylsulfate etc.), solvents (e.g., water, brine, soybean oil etc.),preservatives (e.g., p-hydroxybenzoic acid ester etc.) and the like,which are known to those of ordinary skill in the art.

The intake amount and/or dose of the composition of the presentinvention for preventing atherosclerosis of the present invention variesdepending on the purity of the composition, age, body weight and healthcondition of the subject and the like. However, the intake amount and/ordose is generally 10 mg-10 g, preferably 100 mg-10 g, is preferablygiven or administered to an adult per day for the prevention ofatherosclerosis, which is given once a day or in several portions a day.

Since the composition of the present invention uses plant seeds whichare conventionally used for food and the like (particularly, seed ofsafflower and rapeseed), which are used as a starting material ofcooking oil, the toxicity is extremely low and side effects are scarcelyobserved.

The above written description of the invention provides a manner andprocess of making and using it such that any person skilled in this artis enabled to make and use the same, this enablement being provided inparticular for the subject matter of the appended claims, which make upa part of the original description.

As used herein, the phrases “selected from the group consisting of,”“chosen from,” and the like include mixtures of the specified materials.

Where a numerical limit or range is stated herein, the endpoints areincluded. Also, all values and subranges within a numerical limit orrange are specifically included as if explicitly written out.

The above description is presented to enable a person skilled in the artto make and use the invention, and is provided in the context of aparticular application and its requirements. Various modifications tothe preferred embodiments will be readily apparent to those skilled inthe art, and the generic principles defined herein may be applied toother embodiments and applications without departing from the spirit andscope of the invention. Thus, this invention is not intended to belimited to the embodiments shown, but is to be accorded the widest scopeconsistent with the principles and features disclosed herein.

Having generally described this invention, a further understanding canbe obtained by reference to certain specific examples, which areprovided herein for purposes of illustration only, and are not intendedto be limiting unless otherwise specified.

EXAMPLES Example 1 In Vitro Anti-oxidation Data

Defatted safflower meal (100 g) was mixed with 500 ml of aqueous ethanolcontaining 90 vol % of ethanol and the mixture was warmed with stirringin a hot water bath at 60° C. for 3 hr. Subsequently, the mixture wasfiltered. After filtration, the process was repeated for the solidcontent and the obtained filtrates were combined and concentrated underreduced pressure to yield 60 ml of concentrated solution.

The volume of the concentrated solution was increased to 200 ml bysuspending the contents of the concentrated solution in water. Thesuspension was then washed twice with 120 ml of n-hexane. After washing,the aqueous layer was extracted twice with ethyl acetate (100 ml). Theethyl acetate extract solution was washed with saturated brine, theethyl acetate layer was dried over anhydrous magnesium sulfate, filteredand concentrated under reduced pressure to yield a solid (1.16 g).

Simultaneously, defatted rapeseed meal, soybean meal, soybean germ mealand soybean seed coat, respectively, were subjected to a similartreatment, 1 ml of DMSO was added to 1/10 amount of the above-listedextracts for dissolution and use as samples.

Plasma obtained from a human volunteer (adjusted to density=1.21 (g/ml)with KBr) was subjected to discontinuous density gradient centrifugation(417,000×g, 40 min, 4° C.) (Optima TLX; Beckman Coulter) and an LDL bandwas withdrawn with a syringe. The protein content of the LDL fractionwas measured (BCA protein assay kit; Pierce biotechnology, Inc.), anddiluted with phosphate buffer (PBS) to a final concentration of 100 μgprotein/ml. Thereto 1/100 amount of the above-mentioned sample was addedfollowed by a radical initiator (V70;2,2′-azobis(4-methoxy-2,4-dimethylvaleronitrile)) to a finalconcentration of 1 mM. The absorption at 234 nm (DU640; Beckman Coulter)based on the conjugated diene structure in lipid peroxide wasimmediately monitored for 5 hr. The lag time was calculated according tothe method of Kondo et al. (J. Nutr. Sci. Vitaminol., 43: pp 435-44,1997) based on the obtained lipid peroxide production curve. The effectof each sample on the oxidizability of LDL was evaluated by a relativevalue of the lag time with that of control (solvent alone was added) as100 (FIG. 1). Every sample tended to more or less suppress oxidizabilityof LDL (i.e., extension of ragtime), but rapeseed meal and safflowermeal were particularly strong suppressors of LDL oxidization.

The dilution fold of each sample before mixing with diluted human LDL inthe above-mentioned test was 200-fold for rapeseed meal and safflowermeal, and 50-fold for others. Since these meal extracts are liquid whenconverted to meal before extraction, rapeseed, and safflower mealextracts (200-fold diluted) were at 0.05 g/ml based on rapeseed meal andsafflower meal, while soybean meal, soybean seed coat and soybean germmeal (50-fold diluted) were at 0.2 g/ml based on soybean meal, soybeanseed coat and soybean germ meal. In other words, the rapeseed meal andsafflower meal extract showed stronger antioxidant activity at a lowerconcentration.

Example 2 In Vivo Atherosclerosis Preventive Effect

Extracts of rapeseed meal and safflower meal were prepared as follows.

To defatted rapeseed meal (600 g) 3000 ml of aqueous ethanol containing90 vol % of ethanol was added, and the mixture was warmed and stirred ina hot water bath at 60° C. for 3 hr, followed by filtration. Thisprocess was repeated with the solid content obtained after filtrationand the resultant filtrates were combined and concentrated under reducedpressure to yield 500 ml of concentrated solution. Water was added tothe concentrated solution to produce a suspension at a final volume of1000 ml. The suspension was subsequently washed twice with 500 ml ofn-hexane. The aqueous layer obtained after washing was extracted twicewith ethyl acetate (500 ml) and the ethyl acetate extract solution wasdried over anhydrous magnesium sulfate, filtered and concentrated underreduced pressure to yield an extract (12.5 g).

The defatted safflower meal (600 g) was treated in the same manner asdescribed above resulting in 10.1 g of an extract.

The 9-week-old male apoE knockout mice (apoE(−/−); purchased from TheJackson Laboratory) were divided into three groups of control/rapeseed(rapeseed meal extract administration group)/safflower (safflower mealextract administration group) with 9 mice per group, and each group wasallowed free intake of a feed having ingredients shown in Table 1 for 5weeks. The mice were killed at week 2 (n=6) and week 5 (n=3), a part ofthe aorta from the aortic root to the femoral artery bifurcation wasremoved, and the area of atheromatous plaque (plaque) formed on thevascular inner wall stained with Sudan IV was compared with that of thecontrol group. By 2 weeks' administration, plaque formation tended to besuppressed in the rapeseed group and safflower group as compared to thecontrol group. By comparison of groups after extended administration for3 weeks thereafter, the above-mentioned tendency became stronger (plaquearea: safflower<rapeseed<control), and an effect of suppressingformation of initial lesion of atherosclerosis was exhibited by theseoil plant meal extracts (FIG. 2 and FIG. 3).

Blood was taken from the abdominal vena cava of the mouse killed in theabove-mentioned test. Plasma (adjusted to density of 1.30 (g/ml) withKBr), separated according to conventional methods, was subjected todiscontinuous density gradient centrifugation (417,000×g, 1 hr, 4° C.)(Optima TLX; Beckman Coulter) and a lipoprotein fraction wasfractionated using a fractionator (DGF-U; Hitachi Koki Co., Ltd.). Theprotein content of the VLDL (very low density lipoprotein)—LDL (lowdensity lipoprotein) fraction of each group, confirmed byelectrophoresis (Multigel-lipo; Daiichi Pure Chemicals Co., Ltd), wasmeasured (BCA protein assay kit; Pierce Biotechnology, Inc.).Subsequently, the fraction was diluted with phosphate buffer (PBS) to afinal concentration of 50 fig protein/ml, a radical initiator (V70;2,2′-azobis(4-methoxy-2,4-dimethyl valeronitrile)) was added to a finalconcentration of 250 μM, and the absorption at 234 nm (DU-640; BeckmanCoulter) based on the conjugated diene structure in lipid peroxide at37° C. was immediately initiated. A lipid peroxide production curve wasplotted for each of the administration group and the control group. Theproduction rate and the amount of product were compared (FIG. 4).

Based on the foregoing, it was determined that the lipoprotein fractionsof the rapeseed and safflower administration groups showed lesseraccumulation of lipid peroxide as compared to the control group (namely,less easily oxidized) (safflower<rapeseed<control). TABLE 1 groupIngredients of feed control Normal diet (20% (w/w) vitamin-free casein,66.3% starch, 5% corn oil, 3.5% AIN-93-mineral mixture, 1%AIN-93-vitamin mixture, 0.2% choline chloride, 4% cellulose powder)rapeseed Normal diet + 1.3% (w/w) rapeseed meal extract* safflowerNormal diet + 1.0% (w/w) safflower meal extract**balanced with starch

Example 3

6-7-week-old male apoE knockout mice (purchased from The JacksonLaboratory) were divided into 5 groups: (a) control (Control), (b)serotonin derivative 0.2 wt % administration (p-coumaroylserotonin (CS),feruloylserotonin (FS), 0.1% each) (CS+FS, 0.2%), (c) serotoninderivative 0.4 wt % administration (p-coumaroylserotonin (CS),feruloylserotonin (FS), 0.2% each) (CS+FS, 0.4%), (d) feruloylserotonin(FS) 0.4 wt % administration (FS, 0.4%), and (e) safflower meal extract(SFM) 1 wt % administration (SFM, 1%) with 7-10 mice per group. Eachgroup was allowed free intake of a feed having ingredients shown inTable 2 for 15 weeks.

The safflower meal extract (SFM) used in this Example was preparedaccording to the method described in Example 2. After completion of theadministration period, the mice were killed, the aortic root was slicedand the lipid deposition part (atherosclerosis lesion) was stained withOil Red O. Three slices were prepared for one individual and the samplesmost clearly showing the aortic valve were subjected to image analysis(using WinROOF (MITANI CORPORATION)) and the area of the lesion wasmeasured based on the method of Rajendra et al (J. Lipid Res., 36: pp2320-2328, 1995). The obtained area of the lesion was subjected to ananalysis of variance between respective groups, and when a significantdifference was observed, the average values were compared between groupsby the Scheffe test. While a serotonin derivative (Zhang et al, Chem.Pharm. Bull., 44: pp 874-876, 1996, Kawashima et al, J. InterferonCytokine Res., 18: pp 423-428, 1998), which is a main phenolic substancein safflower meal known to have antioxidant activity andanti-inflammatory activity in vitro, partially suppressed lesionformation in apoE knockout mice, a safflower meal extract (SFM,containing 10-30 wt % of serotonin derivative) was found to suppressstronger than that (FIG. 5). TABLE 2 g (in 1 kg of diet) CS + FS, CS +FS, SFM, FS, composition Control 0.2% 0.4% 1% 0.4% vitamin-free casein200.0 200.0 200.0 200.0 200.0 corn starch 632.5 630.5 628.5 622.5 628.5corn oil 70.0 70.0 70.0 70.0 70.0 mineral mixture 35.0 35.0 35.0 35.035.0 (AIN-93G) vitamin mixture 10.0 10.0 10.0 10.0 10.0 (AIN-93G)choline tartrate 2.5 2.5 2.5 2.5 2.5 cellulose powder 50.0 50.0 50.050.0 50.0 p-coumaroyl- 0.0 1.0 2.0 0.0 0.0 serotonin Feruloyl-serotonin0.0 1.0 2.0 0.0 4.0 safflower meal 0.0 0.0 0.0 10.0 0.0 extract total1000.0 1000.0 1000.0 1000.0 1000.0

Since the composition of the present invention, which is obtained byorganic solvent extraction of defatted plant seed, is a naturallyoccurring material it, shows high safety and almost no side effects. Assuch, based on the results demonstrated above, the resultant compositionof the present invention is an effective preventative ofatherosclerosis. Further, a food and a pharmaceutical compositioncontaining the composition are also effective for preventingatherosclerosis.

Numerous modifications and variations on the present invention arepossible in light of the above teachings. It is, therefore, to beunderstood that within the scope of the accompanying claims, theinvention may be practiced otherwise than as specifically describedherein.

1. (canceled)
 2. The method of claim 18, wherein the plant seed is aseed of safflower.
 3. The method of claim 18, wherein the plant seed isa seed of rapeseed.
 4. The method of claim 18, wherein the organicsolvent extraction is obtained by a process comprising extracting adefatted plant seed with a lower alcohol.
 5. The method of claim 4,wherein said lower alcohol is ethanol or methanol.
 6. The method ofclaim 4, wherein said process further comprises, after said extractingwith a lower alcohol, evaporating said lower alcohol, adding water,extracting an aqueous phase, and washing said aqueous phase with anonpolar solvent.
 7. The method of claim 6, wherein said lower alcoholis ethanol or methanol.
 8. The method of claim 4, wherein said processfurther comprises extracting with an acetate ester after said extractingwith a lower alcohol.
 9. The method of claim 8, wherein said acetateester is selected from the group consisting of ethyl acetate, methylacetate, and propyl acetate.
 10. The method of claim 6, wherein saidnonpolar solvent is n-hexane.
 11. The method of claim 8, wherein saidlower alcohol is ethanol or methanol.
 12. The method of claim 8, whereinsaid process further comprises, after said extracting with a loweralcohol, evaporating said lower alcohol, adding water, extracting anaqueous phase, and washing said aqueous phase with a nonpolar solvent.13. The method of claim 12, wherein said lower alcohol is ethanol ormethanol.
 14. The method of claim 12, wherein said acetate ester isselected from the group consisting of ethyl acetate, methyl acetate, andpropyl acetate.
 15. The method of claim 12, wherein said nonpolarsolvent is n-hexane. 16.-17. (canceled)
 18. A method of preventing oneor more atherosclerotic disease comprising administering to a subject inneed thereof a composition comprising an organic solvent extraction of adefatted plant seed.
 19. The method of claim 18, wherein saidatherosclerotic disease is one or more selected from the groupconsisting of angina pectoris, cardiac infarction, intermittentclaudication, and cerebral infarction.
 20. The method of claim 18,wherein said effective amount ranges from 10 mg to 10 g per day.
 21. Themethod of claim 6, wherein said process further comprises extractingwith an acetate ester after said extracting and washing said aqueousphase with a nonpolar solvent.
 22. The method of claim 21, wherein saidacetate ester is selected from the group consisting of ethyl acetate,methyl acetate, and propyl acetate.
 23. The method of claim 21, whereinsaid nonpolar solvent is n-hexane.